MX2009002802A - 2-aryl-6-phenylimidazo[1,2-î±]pyridine derivatives, preparation thereof and therapeutic use thereof. - Google Patents
2-aryl-6-phenylimidazo[1,2-î±]pyridine derivatives, preparation thereof and therapeutic use thereof.Info
- Publication number
- MX2009002802A MX2009002802A MX2009002802A MX2009002802A MX2009002802A MX 2009002802 A MX2009002802 A MX 2009002802A MX 2009002802 A MX2009002802 A MX 2009002802A MX 2009002802 A MX2009002802 A MX 2009002802A MX 2009002802 A MX2009002802 A MX 2009002802A
- Authority
- MX
- Mexico
- Prior art keywords
- optionally substituted
- cycloalkyl
- aryl
- phenylimidazo
- preparation
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
Abstract
The invention relates to the derivatives of general formula (I) in which: R1 is: a phenyl group or a naphthyl group, it being possible for these two groups to be optionally substituted; R2 and R3 are, independently of one another, a hydrogen atom, a (C1-C6)alkyl, (C3-C7)cycloalkyl or (C3-C7)cycloalkyl(C1-C3) alkylene group, which is optionally substituted; an optionally substituted aryl group; R4 is: a hydrogen atom, a (C1-C6)alkyl, (C3-C7)cycloalkyl or (C3-C7)cycloalkyl(C1-C3) alkylene group, which is optionally substituted; an aryl group optionally substituted with one or more substituents in the form of a base or of an addition salt with an acid.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0608350A FR2906250B1 (en) | 2006-09-22 | 2006-09-22 | DERIVATIVES OF 2-ARYL-6PHENYL-IMIDAZO (1,2-A) PYRIDINES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
PCT/FR2007/001517 WO2008034974A1 (en) | 2006-09-22 | 2007-09-19 | 2-ARYL-6-PHENYLIMIDAZO[1,2-α]PYRIDINE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009002802A true MX2009002802A (en) | 2009-04-01 |
Family
ID=37841968
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009002802A MX2009002802A (en) | 2006-09-22 | 2007-09-19 | 2-aryl-6-phenylimidazo[1,2-î±]pyridine derivatives, preparation thereof and therapeutic use thereof. |
Country Status (44)
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2928922B1 (en) * | 2008-03-21 | 2010-04-23 | Sanofi Aventis | DERIVATIVES OF POLYSUBSTITUTED 2-ARYL-6-PHENYL-IMIDAZO-1,2-A! PYRIDINES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2928924B1 (en) | 2008-03-21 | 2010-04-23 | Sanofi Aventis | POLYSUBSTITUTED DERIVATIVES OF 6-HETEROARYL-IMIDAZO-1,2-A! PYRIDINES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
FR2928921B1 (en) * | 2008-03-21 | 2010-04-23 | Sanofi Aventis | POLYSUBSTITUTED DERIVATIVES OF 2-ARYL-6-PHENYL-IMIDAZO-1,2-A! PYRIDINES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2928923B1 (en) * | 2008-03-21 | 2010-04-23 | Sanofi Aventis | POLYSUBSTITUTED DERIVATIVES OF 2-HETEROARYL-6-PHENYL-IMIDAZO-1,2-A! PYRIDINES, THEIR PREPARATION AND THEIR USE IN THERAPEUTICS |
FR2933609B1 (en) * | 2008-07-10 | 2010-08-27 | Fournier Lab Sa | USE OF INDOLE DERIVATIVES AS NURR-1 ACTIVATORS FOR THE TREATMENT OF PARKINSON'S DISEASE. |
FR2950344B1 (en) * | 2009-09-18 | 2011-11-25 | Sanofi Aventis | 5-PHENYL-PYRAZOLOPYRIDINE DERIVATIVES, THEIR PREPARATION AND THEIR USE IN THERAPEUTICS. |
FR2950345B1 (en) * | 2009-09-18 | 2011-09-23 | Sanofi Aventis | ACETYLENE DERIVATIVES OF 5-PHENYL-PYRAZOLOPYRIDINE, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2953520B1 (en) * | 2009-12-04 | 2011-11-25 | Sanofi Aventis | DIPHENYL-PYRAZOLOPYRIDINE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
MX2015006513A (en) * | 2012-11-29 | 2015-08-14 | Hoffmann La Roche | Imidazopyridine derivatives. |
TWI644899B (en) | 2013-02-04 | 2018-12-21 | 健生藥品公司 | Flap modulators |
US9745328B2 (en) | 2013-02-04 | 2017-08-29 | Janssen Pharmaceutica Nv | Flap modulators |
ES2883565T3 (en) * | 2013-08-02 | 2021-12-09 | Pasteur Institut Korea | Anti-infective compounds |
US10280163B2 (en) | 2015-04-10 | 2019-05-07 | Beigene, Ltd. | 5 or 8-substituted imidazo[1, 5-a] pyridines as indoleamine and/or tryptophane 2, 3-dioxygenases |
ES2928164T3 (en) | 2015-10-19 | 2022-11-15 | Incyte Corp | Heterocyclic compounds as immunomodulators |
TWI763641B (en) | 2015-11-19 | 2022-05-11 | 美商英塞特公司 | Heterocyclic compounds as immunomodulators |
MA55194A (en) | 2015-12-22 | 2022-05-04 | Incyte Corp | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS |
WO2017192961A1 (en) | 2016-05-06 | 2017-11-09 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
MA45116A (en) | 2016-05-26 | 2021-06-02 | Incyte Corp | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS |
UA125391C2 (en) | 2016-06-20 | 2022-03-02 | Інсайт Корпорейшн | Heterocyclic compounds as immunomodulators |
US20180016260A1 (en) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
MA46045A (en) | 2016-08-29 | 2021-04-28 | Incyte Corp | HETEROCYCLIC COMPOUNDS USED AS IMMUNOMODULATORS |
US10882856B2 (en) | 2016-09-24 | 2021-01-05 | Beigene, Ltd. | 5 or 8-substituted imidazo [1,5-a] pyridines as selective inhibitors of indoleamine and/or tryptophane 2,3-dioxygenases |
WO2018119236A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
US20180179179A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
ES2934230T3 (en) | 2016-12-22 | 2023-02-20 | Incyte Corp | Benzooxazole derivatives as immunomodulators |
HRP20221216T1 (en) | 2016-12-22 | 2022-12-23 | Incyte Corporation | Tetrahydro imidazo[4,5-c]pyridine derivatives as pd-l1 internalization inducers |
CN111386114A (en) | 2017-11-25 | 2020-07-07 | 百济神州有限公司 | Novel benzimidazoles as selective inhibitors of indoleamine 2, 3-dioxygenase |
PE20211911A1 (en) | 2018-03-30 | 2021-09-28 | Incyte Corp | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS |
MD3790877T2 (en) | 2018-05-11 | 2023-08-31 | Incyte Corp | Tetrahydro-imidazo[4,5-c]pyridine derivatives as pd-l1 immunomodulators |
WO2021030162A1 (en) | 2019-08-09 | 2021-02-18 | Incyte Corporation | Salts of a pd-1/pd-l1 inhibitor |
KR20220075382A (en) | 2019-09-30 | 2022-06-08 | 인사이트 코포레이션 | Pyrido[3,2-d]pyrimidine compounds as immunomodulators |
AU2020385113A1 (en) | 2019-11-11 | 2022-05-19 | Incyte Corporation | Salts and crystalline forms of a PD-1/PD-L1 inhibitor |
US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
CA3200844A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process for making a pd-1/pd-l1 inhibitor and salts and crystalline forms thereof |
US11760756B2 (en) | 2020-11-06 | 2023-09-19 | Incyte Corporation | Crystalline form of a PD-1/PD-L1 inhibitor |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
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JP4041624B2 (en) * | 1999-07-21 | 2008-01-30 | 三井化学株式会社 | Organic electroluminescence device |
US6489337B1 (en) * | 2000-03-31 | 2002-12-03 | Ortho-Mcneil Pharmaceutical, Inc. | Method for treating histamine H3 receptor-mediated disorders with 2- or 3-aryl substituted imidazo[1,2-a] pyridines |
GB0119911D0 (en) * | 2001-08-15 | 2001-10-10 | Novartis Ag | Organic Compounds |
AU2003295332B2 (en) * | 2002-09-19 | 2007-01-18 | Merck Sharp & Dohme Corp. | Imidazopyridines as cyclin dependent kinase inhibitors |
GB0303503D0 (en) * | 2003-02-14 | 2003-03-19 | Novartis Ag | Organic compounds |
CN1930159A (en) * | 2004-03-08 | 2007-03-14 | 北卡罗来纳大学查珀尔希尔分校 | Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8,-tetrahydro-imidazo[1,2,-a]pyridines as antiprotozoal agents |
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2006
- 2006-09-22 FR FR0608350A patent/FR2906250B1/en active Active
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2007
- 2007-09-13 TW TW096134253A patent/TWI381837B/en not_active IP Right Cessation
- 2007-09-19 MY MYPI20091157A patent/MY145603A/en unknown
- 2007-09-19 PL PL07848251T patent/PL2069342T3/en unknown
- 2007-09-19 SI SI200730316T patent/SI2069342T1/en unknown
- 2007-09-19 JP JP2009528752A patent/JP5336378B2/en not_active Expired - Fee Related
- 2007-09-19 DK DK07848251.0T patent/DK2069342T3/en active
- 2007-09-19 NZ NZ575337A patent/NZ575337A/en not_active IP Right Cessation
- 2007-09-19 ME MEP-2009-107A patent/ME00615B/en unknown
- 2007-09-19 UA UAA200903928A patent/UA95976C2/en unknown
- 2007-09-19 AU AU2007298856A patent/AU2007298856B2/en not_active Ceased
- 2007-09-19 DE DE602007006525T patent/DE602007006525D1/en active Active
- 2007-09-19 PT PT07848251T patent/PT2069342E/en unknown
- 2007-09-19 AR ARP070104136A patent/AR062897A1/en not_active Application Discontinuation
- 2007-09-19 AT AT07848251T patent/ATE467633T1/en active
- 2007-09-19 ZA ZA200901551A patent/ZA200901551B/en unknown
- 2007-09-19 MX MX2009002802A patent/MX2009002802A/en active IP Right Grant
- 2007-09-19 ES ES07848251T patent/ES2345016T3/en active Active
- 2007-09-19 CA CA2662848A patent/CA2662848C/en not_active Expired - Fee Related
- 2007-09-19 BR BRPI0718517-0A patent/BRPI0718517A2/en active Search and Examination
- 2007-09-19 EP EP07848251A patent/EP2069342B1/en active Active
- 2007-09-19 CN CN2007800352403A patent/CN101516881B/en not_active Expired - Fee Related
- 2007-09-19 EA EA200970311A patent/EA017442B1/en not_active IP Right Cessation
- 2007-09-19 RS RSP-2010/0356A patent/RS51412B/en unknown
- 2007-09-19 KR KR1020097005741A patent/KR101470039B1/en not_active IP Right Cessation
- 2007-09-19 WO PCT/FR2007/001517 patent/WO2008034974A1/en active Application Filing
- 2007-09-20 PE PE2007001266A patent/PE20080671A1/en not_active Application Discontinuation
- 2007-09-20 JO JO2007401A patent/JO2643B1/en active
- 2007-09-21 CL CL200702733A patent/CL2007002733A1/en unknown
- 2007-09-21 UY UY30603A patent/UY30603A1/en not_active Application Discontinuation
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2009
- 2009-02-26 CR CR10643A patent/CR10643A/en unknown
- 2009-03-02 IL IL197352A patent/IL197352A/en not_active IP Right Cessation
- 2009-03-05 GT GT200900049A patent/GT200900049A/en unknown
- 2009-03-10 TN TN2009000081A patent/TN2009000081A1/en unknown
- 2009-03-18 HN HN2009000502A patent/HN2009000502A/en unknown
- 2009-03-19 US US12/407,449 patent/US7915284B2/en not_active Expired - Fee Related
- 2009-03-19 SV SV2009003193A patent/SV2009003193A/en active IP Right Grant
- 2009-03-19 NI NI200900037A patent/NI200900037A/en unknown
- 2009-03-19 CO CO09028759A patent/CO6160308A2/en unknown
- 2009-04-16 MA MA31788A patent/MA30792B1/en unknown
- 2009-04-20 NO NO20091562A patent/NO20091562L/en not_active Application Discontinuation
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2010
- 2010-02-22 HK HK10101842.6A patent/HK1135388A1/xx not_active IP Right Cessation
- 2010-07-20 CY CY20101100678T patent/CY1110232T1/en unknown
- 2010-07-23 HR HR20100408T patent/HRP20100408T1/en unknown
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